A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417173



Internal ID21074726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116732884..116742488hg38UCSC Ensembl
chr8:117745123..117754727hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg389605
hg199605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163721
Samples
Known GenesEIF3H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417173
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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